| 怑楌 |
丗 |
| 2002擭12寧乣2006擭02寧 |
丗 |
攷巑尋媶堳乮Helen Hay Whitney postdoctoral fellow乯, Department of Chemistry and Chemical Biology,丂Harvard University乮David R. Liu嫵庼乯 |
| 2006擭03寧乣08寧 |
丗 |
尋媶堳,丂Howard Hughes Medical Institute, Department of Chemistry and Chemical Biology, Harvard University乮David R. Liu嫵庼乯 |
| 2006擭09寧乣10寧 |
丗 |
彆庤丄搶杒戝妛戝妛堾棟妛尋媶壢壔妛愱峌 |
| 2006擭10寧乣2007擭03寧 |
丗 |
摿擟彆嫵庼丄搶嫗擾岺戝妛嫟惗壢妛媄弍尋媶堾 |
| 2007擭04寧乣 |
丗 |
摿擟弝嫵庼丄摨忋 |
|
| 妛楌 |
丗 |
| 1996擭03寧 |
丗 |
搶嫗戝妛棟妛晹壔妛壢懖嬈乮媖榓晇嫵庼乯 |
| 1996擭09寧 |
丗 |
Department of Chemistry, Princeton University,丂 戝妛堾擖妛 |
| 2003擭06寧 |
丗 |
Department of Chemistry, Princeton University, Ph.D. in Chemistry 庢摼乮Daniel Kahne嫵庼乯 |
|
| 庴徿楌 |
丗 |
| 1996擭03寧 |
丗 |
掗恖媣懞彠妛嬥乮暷崙棷妛偺偨傔帿戅乯 |
| 2000擭03寧 |
丗 |
The Merck-Pachett Summer Award |
| 2002擭12寧 |
丗 |
The Helen Hay Whitney Foundation Postdoctoral Fellowship |
| 2005擭08寧 |
丗 |
戞屲夞揤慠暔壔妛択榖夛彠椼徿 |
|
| 庡側榑暥丒夝愢 |
丗 |
| 丒 |
Sakurai, K., Schubert, C., Kahne, D. 乬Crystallographic Analysis of an 8-mer p53 Peptide Analogue Complexed with MDM2乭 J. Am. Chem. Soc. 2006, 128, 11000-11001. |
| 丒 |
Sakurai, K., Snyder, T. M., Liu, D. R. 乬DNA-templated Functional Group Transformations Enable Sequence-Programmed Synthesis Using Small Molecule Reagents乭 J. Am. Chem. Soc. 2005, 127, 1660-1661. |
| 丒 |
Sakurai, K., Chung, H. S., Kahne, D. 乬Use of a Retroinverso p53 Peptide as an Inhibitor of MDM2乭 J. Am. Chem. Soc. 2004, 126, 16288-16289. |
| 丒 |
Kanan, M.W., Rozenman, M. M., Sakurai, K., Snyder, T. M., Liu. D. R. 乬Reaction Discovery Enabled by DNA-Templated Synthesis and In Vitro Selection乭 Nature 2004, 431, 545-549. |
| 丒 |
Gildersleeve, J., Smith, A., Sakurai, K., Raghavan, S., Kahne, D. 乬Scavenging Byproducts in the Sulfoxide Glycosylation Reaction: Application to the Synthesis of Ciclamycin 0乭 J. Am. Chem. Soc. 1999, 121, 6176-6182. |
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